{"title":"Synthesis of Mimicking Plant Cell Wall-Like Anti-Swelling Hydrogels Based on a “Bottom-Up” Strategy and Their Application in Osmotic Energy Harvesting","authors":"Zhuowen Zhang, Zhen Wang, Xinrui Wang, Xiaomeng Zhou, Xinjian Zhang, Jianing Wang","doi":"10.1002/adfm.202502946","DOIUrl":null,"url":null,"abstract":"<p>Osmotic energy harvesting via reverse electrodialysis (RED) presents a promising approach for converting salinity gradient energy into usable power. However, the broad implementation of this technology faces significant barriers, including the inherent instability of conventional ion-selective membranes, the intricacy of fabrication techniques, and unresolved environmental challenges. This hydrogel combines the structural and adhesive properties of carboxymethyl cellulose (CMC) and double-bond lignosulfonate sodium (DLS) to enhance antiswelling performance. DLS is functionalized through a hydroxyl-alkyne click reaction, transforming it into a highly reactive supramolecule. Simultaneously, CMC is integrated into the gel network using a choline chloride/acrylic acid deep eutectic solvent, where acrylic acid acts as both a hydrogen bond donor and a polymerizable monomer. The resulting hydrogel demonstrates remarkable ion selectivity and efficient osmotic energy harvesting, achieving an ultralow swelling rate of 0.385, an output power density of 10.10 W m<sup>−</sup><sup>2</sup> (double the commercial benchmark of 5.0 W m<sup>−</sup><sup>2</sup>), and an ion selectivity of 99.10%. This study underscores the potential of biomass-based hydrogels as sustainable, high-performance materials for osmotic energy harvesting, offering a viable pathway for next-generation energy technologies.</p>","PeriodicalId":112,"journal":{"name":"Advanced Functional Materials","volume":"35 34","pages":""},"PeriodicalIF":19.0000,"publicationDate":"2025-03-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Advanced Functional Materials","FirstCategoryId":"88","ListUrlMain":"https://advanced.onlinelibrary.wiley.com/doi/10.1002/adfm.202502946","RegionNum":1,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0
Abstract
Osmotic energy harvesting via reverse electrodialysis (RED) presents a promising approach for converting salinity gradient energy into usable power. However, the broad implementation of this technology faces significant barriers, including the inherent instability of conventional ion-selective membranes, the intricacy of fabrication techniques, and unresolved environmental challenges. This hydrogel combines the structural and adhesive properties of carboxymethyl cellulose (CMC) and double-bond lignosulfonate sodium (DLS) to enhance antiswelling performance. DLS is functionalized through a hydroxyl-alkyne click reaction, transforming it into a highly reactive supramolecule. Simultaneously, CMC is integrated into the gel network using a choline chloride/acrylic acid deep eutectic solvent, where acrylic acid acts as both a hydrogen bond donor and a polymerizable monomer. The resulting hydrogel demonstrates remarkable ion selectivity and efficient osmotic energy harvesting, achieving an ultralow swelling rate of 0.385, an output power density of 10.10 W m−2 (double the commercial benchmark of 5.0 W m−2), and an ion selectivity of 99.10%. This study underscores the potential of biomass-based hydrogels as sustainable, high-performance materials for osmotic energy harvesting, offering a viable pathway for next-generation energy technologies.
通过反电渗析(RED)的渗透能量收集提供了一种将盐度梯度能量转化为可用能量的有前途的方法。然而,该技术的广泛应用面临着巨大的障碍,包括传统离子选择膜的固有不稳定性、制造技术的复杂性以及未解决的环境挑战。这种水凝胶结合了羧甲基纤维素(CMC)和双键木质素磺酸钠(DLS)的结构和粘合性能,以增强抗膨胀性能。DLS通过羟基炔咔嗒反应被功能化,转化为高活性的超分子。同时,CMC使用氯化胆碱/丙烯酸深共熔溶剂集成到凝胶网络中,其中丙烯酸既充当氢键供体,又充当可聚合单体。所制备的水凝胶具有显著的离子选择性和高效的渗透能量收集,其溶胀率为0.385,输出功率密度为10.10 W m−2(是商用基准5.0 W m−2的两倍),离子选择性为99.10%。这项研究强调了生物质基水凝胶作为可持续、高性能渗透能量收集材料的潜力,为下一代能源技术提供了一条可行的途径。
期刊介绍:
Firmly established as a top-tier materials science journal, Advanced Functional Materials reports breakthrough research in all aspects of materials science, including nanotechnology, chemistry, physics, and biology every week.
Advanced Functional Materials is known for its rapid and fair peer review, quality content, and high impact, making it the first choice of the international materials science community.